P
US6506559B1ExpiredUtilityPatentIndex 98

Genetic inhibition by double-stranded RNA

Assignee: UNIV MASSACHUSETTSPriority: Dec 23, 1997Filed: Dec 18, 1998Granted: Jan 14, 2003
Est. expiryDec 23, 2017(expired)· nominal 20-yr term from priority
Inventors:FIRE ANDREWKOSTAS STEPHENMONTGOMERY MARYTIMMONS LISAXU SIQUNTABARA HIROAKIDRIVER SAMUEL EMELLO CRAIG C
C12N 2310/53C12N 15/8218C12N 15/85C12N 15/113A61K 31/713C12N 15/8285A01K 2227/703C12N 2310/50A61P 43/00A61P 35/00A61P 35/02A61K 31/7105C12N 2310/14C12N 2310/11A01K 2217/05C12N 2310/321
98
PatentIndex Score
3,119
Cited by
148
References
22
Claims

Abstract

A process is provided of introducing an RNA into a living cell to inhibit gene expression of a target gene in that cell. The process may be practiced ex vivo or in vivo. The RNA has a region with double-stranded structure. Inhibition is sequence-specific in that the nucleotide sequences of the duplex region of the RNA and of a portion of the target gene are identical. The present invention is distinguished from prior art interference in gene expression by antisense or triple-strand methods.

Claims

exact text as granted — not AI-modified
We claim:  
     
       1. A method to inhibit expression of a target gene in a cell in vitro comprising introduction of a ribonucleic acid (RNA) into the cell in an amount sufficient to inhibit expression of the target gene, wherein the RNA is a double-stranded molecule with a first strand consisting essentially of a ribonucleotide sequence which corresponds to a nucleotide sequence of the target gene and a second strand consisting essentially of a ribonucleotide sequence which is complementary to the nucleotide sequence of the target gene, wherein the first and the second ribonucleotide strands are separate complementary strands that hybridize to each other to form said double-stranded molecule, and the double-stranded molecule inhibits expression of the target gene. 
     
     
       2. The method of  claim 1  in which the target gene is a cellular gene. 
     
     
       3. The method of  claim 1  in which the target gene is an endogenous gene. 
     
     
       4. The method of  claim 1  in which the target gene is a transgene. 
     
     
       5. The method of  claim 1  in which the target gene is a viral gene. 
     
     
       6. The method of  claim 1  in which the cell is from an animal. 
     
     
       7. The method of  claim 1  in which the cell is from a plant. 
     
     
       8. The method of  claim 6  in which the cell is from an invertebrate animal. 
     
     
       9. The method of  claim 8  in which the cell is from a nematode. 
     
     
       10. The method of  claim 1  in which the first ribonucleotide sequence comprises at least 25 bases which correspond to the target gene and the second ribonucleotide sequence comprises at least 25 bases which are complementary to the nucleotide sequence of the target gene. 
     
     
       11. The method of  claim 1  in which the target gene expression is inhibited by at least 10%. 
     
     
       12. A method to inhibit expression of a target gene in an invertebrate organism comprising: 
       (a) providing an invertebrate organism containing a target cell, wherein the target cell contains the target gene and the target cell is susceptible to RNA interference, and the target gene is expressed in the target cell;  
       (b) contacting said invertebrate organism with a ribonucleic acid (RNA), wherein the RNA is a double-stranded molecule with a first strand consisting essentially of a ribonucleotide sequence which corresponds to a nucleotide sequence of the target gene and a second strand consisting essentially of a ribonucleotide sequence which is complementary to the nucleotide sequence of the target gene, wherein the first and the second ribonucleotide sequences are separate complementary strands that hybridize to each other to form the double-stranded molecule; and  
       (c) introducing the RNA into the target cell, thereby inhibiting expression of the target gene.  
     
     
       13. The method of  claim 12  in which the organism is a nematode. 
     
     
       14. The method of  claim 13  in which a formulation comprised of the RNA is applied on or adjacent to a plant, and disease associated with nematode infection of the plant is thereby reduced. 
     
     
       15. The method of  claim 12  in which said double-stranded ribonucleic acid structure is at least 25 bases in length and each of the ribonucleic acid strands is able to specifically hybridize to a deoxyribonucleic acid strand of the target gene over the at least 25 bases. 
     
     
       16. The method of  claim 12  in which the expression of the target gene is inhibited by at least 10%. 
     
     
       17. The method of  claim 12  in which the RNA is introduced within a body cavity of the organism and outside the target cell. 
     
     
       18. The method of  claim 12  in which the RNA is introduced by extracellular injection into the organism. 
     
     
       19. The method of  claim 12  in which the organism is contacted with the RNA by feeding the organism food containing the RNA. 
     
     
       20. The method of  claim 19  in which the food comprises a genetically-engineered host transcribing the RNA. 
     
     
       21. The method of  claim 12  in which at least one strand of the RNA is produced by transcription of an expression construct. 
     
     
       22. The method of  claim 21  in which the organism is a nematode and the expression construct is contained in a plant, and disease associated with nematode infection of the plant is thereby reduced.

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